Canonical Allele Identifier: CA658984108

Gene: FGF8

Linked Data

• dbSNP Id: rs1213901955
• gnomAD v4: 10-101775033-TCCC-T
• MyVariant Identifiers: chr10:g.103534791_103534793del (hg19) ; chr10:g.101775034_101775036del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101775036_101775038del , CM000672.2:g.101775036_101775038del	GRCh38
NC_000010.10:g.103534793_103534795del , CM000672.1:g.103534793_103534795del	GRCh37
NC_000010.9:g.103524783_103524785del	NCBI36
NG_007151.1:g.6035_6037del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.156+94_156+96del MANE Select	ENSP00000321797.2:n.156+94_156+96del
ENST00000618991.5:c.-123-157_-123-155del	ENSP00000484420.1:n.-123-157_-123-155del
ENST00000344255.8:c.156+94_156+96del	ENSP00000340039.3:n.156+94_156+96del
ENST00000320185.6:c.156+94_156+96del	ENSP00000321797.2:n.156+94_156+96del
ENST00000344255.7:c.156+94_156+96del	ENSP00000340039.3:n.156+94_156+96del
ENST00000346714.7:c.70-157_70-155del	ENSP00000344306.3:n.70-157_70-155del
ENST00000347978.2:c.70-124_70-122del	ENSP00000321945.2:n.70-124_70-122del
ENST00000469792.6:c.*154-157_*154-155del	ENSP00000473299.1:n.*154-157_*154-155del
ENST00000485728.1:n.33-124_33-122del
ENST00000618991.4:c.-123-157_-123-155del	ENSP00000484420.1:n.-123-157_-123-155del
NM_001206389.1:c.-123-157_-123-155del	NP_001193318.1:n.-123-157_-123-155del
NM_006119.4:c.70-124_70-122del	NP_006110.1:n.70-124_70-122del
NM_033163.3:c.156+94_156+96del	NP_149353.1:n.156+94_156+96del
NM_033164.3:c.156+94_156+96del	NP_149354.1:n.156+94_156+96del
NM_033165.3:c.70-157_70-155del	NP_149355.1:n.70-157_70-155del
XM_011539509.1:c.79-124_79-122del	XP_011537811.1:n.79-124_79-122del
NM_006119.5:c.70-124_70-122del	NP_006110.1:n.70-124_70-122del
NM_033163.4:c.156+94_156+96del	NP_149353.1:n.156+94_156+96del
NM_033164.4:c.156+94_156+96del	NP_149354.1:n.156+94_156+96del
NM_033165.4:c.70-157_70-155del	NP_149355.1:n.70-157_70-155del
NM_001206389.2:c.-123-157_-123-155del	NP_001193318.1:n.-123-157_-123-155del
NM_006119.6:c.70-124_70-122del	NP_006110.1:n.70-124_70-122del
NM_033163.5:c.156+94_156+96del MANE Select	NP_149353.1:n.156+94_156+96del
NM_033165.5:c.70-157_70-155del	NP_149355.1:n.70-157_70-155del